Evidence map›Paper›PMID 1974122›Full record

ReviewAmerican journal of human genetics1990

The fragile X: progress toward solving the puzzle.

W T Brown

Abstract readReview
In one paragraph

Review in American journal of human genetics, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Review
  3. Article
  4. The FRAXE Syndrome: is it time for routine screening?American journal of human genetics · 1996
    Article
  5. Article
  6. Article
  7. Origins of the fragile X syndrome mutation.Journal of medical genetics · 1993
    Article
  8. Review
  9. Article
  10. Physical map of human Xq27-qter: localizing the region of the fragile X mutation.Proceedings of the National Academy of Sciences of the United States of America · 1991
    Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

W T BrownDepartment of Pediatrics, North Shore University Hospital-Cornell University Medical College, Manhasset, NY 11030.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

FemaleFetal DiseasesFragile X SyndromeHumansMalePolymorphism, Restriction Fragment LengthPregnancyPrenatal DiagnosisRestriction MappingSex Chromosome Aberrations

Identifiers

PMID1974122
PMCPMC1683734

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.